Yazar "Cabuk, Feryal" için listeleme
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Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstruction
Jenkins, Dagan; Caubit, Xavier; Dimovski, Aleksandar; Matevska, Nadica; Lye, Claire M.; Cabuk, Feryal; Woolf, Adrian S. (Oxford Univ Press, 2010)Methods. Given the phenotype of Tshz3 mutant mice, we considered that Teashirt genes, which code for a family of transcription factors, might represent candidate genes for human PUJO. To evaluate this possibility, we used ... -
Association of MTHFR A1298C polymorphism with conotruncal heart disease
Kocakap, Beyza D. Sayin; Sanli, Cihat; Cabuk, Feryal; Koc, Murat; Kutsal, Ali (Cambridge Univ Press, 2015)Congenital heart diseases are common congenital anomalies with 1% prevalence worldwide and are associated with significant childhood morbidity and mortality. Among a wide range of aetiologically heterogeneous conditions, ... -
The association of paraoxonase 1 gene L55M polymorphism with the extent and severity of coronary artery disease in the Turkish population and its dependence on gender
Kocakap, Derya Beyza Sayin; Dogru, Mehmet Tolga; Simsek, Vedat; Cabuk, Feryal; Yildirim, Nesligul; Celik, Yunus; Erdem, Solmaz (Turkish Soc Cardiology, 2016)Objective: Coronary artery disease (CAD) is a common, complex, and progressive disorder characterized by the accumulation of lipids and fibrous elements in the arteries. It is one of the leading causes of death in ... -
The frequency of Familial Mediterranean fever gene mutations and genotypes at Kirikkale and comparison with the mean of regional MEFV mutation frequency of Turkey
Kocakap, Derya Beyza Sayin; Gunel-Ozcan, Aysen; Cabuk, Feryal; Ensari, Cuneyt (Springer, 2014)In this study we have retrospectively analysed the mutation spectrum of the 351 Familial Mediterranean fever patients referred to KA +/- rA +/- kkale University Faculty of Medicine, Department of Medical Genetics Laboratory ...
